Rao Vagicherla Kameshwara, Rao Madharam Sudershan, Jain Navin, Panwar Jitendra, Kumar Anil
Department of Chemistry, Birla Institute of Technology and Science, Pilani 333 031, Rajasthan, India.
Org Med Chem Lett. 2011 Sep 27;1(1):10. doi: 10.1186/2191-2858-1-10.
An efficient, one-pot synthesis was developed for 3-aminoalkylated indoles by three-component coupling reaction of aldehydes, N-methylanilines, and indoles using AgOTf as a catalyst. A series of twenty 3-aminoalkylated indoles was evaluated for their antibacterial activities against both Gram negative and Gram positive bacteria. Compounds 4b and 4r showed good antibacterial activity against both Gram positive and Gram negative strains. However, inversing the property of substituent (from 4r to 4q) resulted in the significant fall in the magnitude of antibacterial activity against Escherichia coli.
通过醛、N-甲基苯胺和吲哚的三组分偶联反应,以三氟甲磺酸银为催化剂,开发了一种高效的一锅法合成3-氨基烷基化吲哚的方法。对一系列20种3-氨基烷基化吲哚进行了针对革兰氏阴性菌和革兰氏阳性菌的抗菌活性评估。化合物4b和4r对革兰氏阳性菌和革兰氏阴性菌菌株均表现出良好的抗菌活性。然而,取代基性质的反转(从4r到4q)导致对大肠杆菌的抗菌活性强度显著下降。